Product image of Laramo (Lacosamide) supplied by GNH India

Laramo

Active Ingredient:
Lacosamide
Origin:
EU

Laramo (Lacosamide)

Lacosamide, the active ingredient in Laramo, is a sodium channel blocker presented as a tablet/oral for oral use. It is used to treat partial‑onset seizures in patients with epilepsy.
GNH India supplies Laramo as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Ardez Pharma

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Indications & Clinical Uses

Lacosamide is an anticonvulsant that acts on neuronal sodium channels to control seizure activity.

  • Partial‑onset seizures (epilepsy): reduces seizure frequency as adjunctive therapy in focal epilepsy.
  • Adjunctive therapy for refractory focal epilepsy: provides additional seizure control when other antiepileptics are insufficient.
  • Epilepsy in adults and children (≥4 years): approved for use as part of a comprehensive seizure management plan.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, stabilizing hyperexcitable neuronal membranes and limiting repetitive neuronal firing. By selectively targeting the slow inactivation pathway, it reduces the propagation of epileptiform activity without markedly affecting normal neuronal conduction.

Side Effects

Lacosamide may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Dizziness: transient sensation of light‑headedness or imbalance.
  • Nausea: mild to moderate gastrointestinal upset.
  • Headache: occasional tension‑type headache.
  • Fatigue: feeling unusually tired or weak.
  • Blurred vision: temporary visual disturbances.
  • Diplopia: double vision, especially at higher doses.

Serious or Rare Side Effects

  • Cardiac conduction abnormalities: PR‑interval prolongation or arrhythmias.
  • Suicidal ideation: emergence of depressive thoughts or behaviors.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hypersensitivity: rash, angioedema, or anaphylaxis.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Respiratory depression: especially when combined with other CNS depressants.

Precautions & Warnings

When prescribing or dispensing lacosamide, consider the following safety measures.

  • Renal impairment: assess kidney function and adjust dosing if necessary.
  • Hepatic impairment: monitor liver enzymes and use caution in patients with liver disease.
  • Cardiac conduction disorders: avoid in patients with known PR‑interval prolongation or arrhythmias.
  • Pregnancy: safety not established; weigh potential benefits against risks.
  • Concomitant CNS depressants: monitor for additive sedation or respiratory effects.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lacosamide can interact with several drug classes; awareness of interaction severity guides clinical decisions.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase lacosamide plasma levels.
  • Strong CYP3A4 inducers (e.g., carbamazepine, phenytoin): may reduce therapeutic concentrations.
  • Class III antiarrhythmics (e.g., amiodarone): additive effects on cardiac conduction.

Moderate Interactions (Monitor Closely)

  • Other antiepileptic drugs (e.g., valproate, phenobarbital): may require dose adjustments.
  • Alcohol: potentiates central nervous system depression.
  • Tricyclic antidepressants: increased risk of dizziness and cardiac effects.

Frequently Asked Questions

Laramo contains the active ingredient lacosamide, which is prescribed to treat partial‑onset seizures in patients with epilepsy. It is used as an adjunctive therapy to help reduce the frequency of focal seizures when other antiepileptic medications do not provide adequate control.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes. This stabilizes hyperexcitable neurons, limits repetitive firing, and thereby reduces the propagation of seizure activity without significantly affecting normal neuronal conduction.

The appropriate dose of Laramo is determined by the prescribing clinician based on the patient’s age, weight, renal and hepatic function, and response to therapy. Dosage adjustments are individualized and should follow the prescriber’s instructions.

Safety data for lacosamide in pregnancy and lactation are limited. The medication should only be used if the potential benefit justifies the potential risk to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives and risks with their healthcare provider.

To order Laramo, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any necessary import documentation.

Lacosamide’s unique mechanism—enhancing slow sodium‑channel inactivation—differs from many traditional antiepileptics that target fast inactivation. This can provide additional seizure control for patients who have not responded to other agents, while offering a generally favorable tolerability profile compared with some older drugs.

Laramo should be stored at ambient temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and avoid storing it in bathrooms or other humid environments.

Laramo is taken orally, usually with or without food, as directed by the prescriber. The tablets should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed.

Serious risks include cardiac conduction abnormalities such as PR‑interval prolongation, potential suicidal thoughts or behaviors, severe skin reactions like Stevens‑Johnson syndrome, and rare cases of hepatic dysfunction. Patients should be monitored regularly for these events, especially during treatment initiation and dose changes.

Laramo is contraindicated in patients with known hypersensitivity to lacosamide or any of its excipients, and it should be avoided in individuals with significant cardiac conduction disorders, such as marked PR‑interval prolongation, unless closely monitored by a cardiologist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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